Research Faculty of Agriculture, Hokkaido University, Sapporo, Hokkaido, Japan.
Hokkaido Agricultural Research Center, National Agriculture and Food Research Organization, Memuro, Hokkaido, Japan.
PLoS One. 2023 Aug 8;18(8):e0285430. doi: 10.1371/journal.pone.0285430. eCollection 2023.
Heteroplasmy, the coexistence of multiple mitochondrial DNA (mtDNA) sequences in a cell, is well documented in plants. Next-generation sequencing technology (NGS) has made it feasible to sequence entire genomes. Thus, NGS has the potential to detect heteroplasmy; however, the methods and pitfalls in heteroplasmy detection have not been fully investigated and identified. One obstacle for heteroplasmy detection is the sequence homology between mitochondrial-, plastid-, and nuclear DNA, of which the influence of nuclear DNA segments homologous to mtDNA (numt) need to be minimized. To detect heteroplasmy, we first excluded nuclear DNA sequences of sugar beet (Beta vulgaris) line EL10 from the sugar beet mtDNA sequence. NGS reads were obtained from single plants of sugar beet lines NK-195BRmm-O and NK-291BRmm-O and mapped to the unexcluded mtDNA regions. More than 1000 sites exhibited intra-individual polymorphism as detected by genome browsing analysis. We focused on a 309-bp region where 12 intra-individual polymorphic sites were closely linked to each other. Although the existence of DNA molecules having variant alleles at the 12 sites was confirmed by PCR amplification from NK-195BRmm-O and NK-291BRmm-O, these variants were not always called by six variant-calling programs, suggesting that these programs are inappropriate for intra-individual polymorphism detection. When we changed the nuclear DNA reference, a numt absent from EL10 was found to include the 309-bp region. Genetic segregation of an F2 population from NK-195BRmm-O x NK-291BRmm-O supported the numt origin of the variant alleles. Using four references, we found that numt detection exhibited reference dependency, and extreme polymorphism of numts exists among sugar beet lines. One of the identified numts absent from EL10 is also associated with another intra-individual polymorphic site in NK-195mm-O. Our data suggest that polymorphism among numts is unexpectedly high within sugar beets, leading to confusion about the true degree of heteroplasmy.
异质性,即细胞中存在多种线粒体 DNA(mtDNA)序列,在植物中已有充分的记载。下一代测序技术(NGS)使得对整个基因组进行测序成为可能。因此,NGS 有可能检测到异质性;然而,异质性检测的方法和陷阱尚未得到充分的研究和确定。异质性检测的一个障碍是线粒体、质体和核 DNA 之间的序列同源性,其中需要最小化与 mtDNA 同源的核 DNA 片段(numt)的影响。为了检测异质性,我们首先从甜菜 mtDNA 序列中排除了甜菜(Beta vulgaris)EL10 品系的核 DNA 序列。从甜菜品系 NK-195BRmm-O 和 NK-291BRmm-O 的单个植株中获得 NGS 读取,并将其映射到未排除的 mtDNA 区域。通过基因组浏览分析,发现 1000 多个位点表现出个体内多态性。我们将重点放在一个 309bp 的区域,该区域的 12 个个体内多态性位点彼此紧密相连。尽管通过从 NK-195BRmm-O 和 NK-291BRmm-O 中进行 PCR 扩增证实了这些位点存在具有变体等位基因的 DNA 分子,但这些变体并不总是被六个变体调用程序调用,这表明这些程序不适合个体内多态性检测。当我们改变核 DNA 参考时,发现一个不存在于 EL10 中的 numt 包含了 309bp 区域。来自 NK-195BRmm-O x NK-291BRmm-O 的 F2 群体的遗传分离支持了变体等位基因的 numt 起源。使用四个参考,我们发现 numt 检测表现出参考依赖性,并且甜菜品系之间存在极端的 numt 多态性。从 EL10 中鉴定出的 numt 之一也与 NK-195mm-O 中的另一个个体内多态性位点相关。我们的数据表明,甜菜内部 numt 之间的多态性出乎意料地高,导致对真正异质性程度的混淆。